Canonical Allele Identifier: CA2493479003

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015356G= , CM000664.2:g.21015356G=	GRCh38
NC_000002.11:g.21238228G= , CM000664.1:g.21238228G=	GRCh37
NC_000002.10:g.21091733G=	NCBI36
NG_011793.1:g.33718C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2814+14C=	ENSP00000501110.2:n.*2814+14C=
ENST00000673882.2:c.*2603+14C=	ENSP00000501253.2:n.*2603+14C=
ENST00000673739.1:c.3222+14C=	ENSP00000501110.1:n.3222+14C=
ENST00000673882.1:c.3011+14C=	ENSP00000501253.1:n.3011+14C=
ENST00000233242.5:c.3508+14C= MANE Select	ENSP00000233242.1:n.3508+14C=
ENST00000616098.4:c.3508+14C=	ENSP00000477990.1:n.3508+14C=
NM_000384.2:c.3508+14C=	NP_000375.2:n.3508+14C=
XM_011532809.1:c.3508+14C=	XP_011531111.1:n.3508+14C=
NM_000384.3:c.3508+14C= MANE Select	NP_000375.3:n.3508+14C=